Nephrostomy catheter - UK MHRA Medical Device Registration

Nephrostomy catheter is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96056. The device is manufactured by UreSil, LLC from United States, classified as System or Procedure Pack. The authorized representative in the UK is Emergo Consulting (UK) Limited .

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System or Procedure Pack

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Nephrostomy catheter

MHRA Device ID: 96056•Ref: 96056

Device Type

System or Procedure Pack

Devices

Nephrostomy catheter

Type

System or Procedure Pack

Date Registered

Nov 26, 2024

Last Updated

Jul 3, 2024

Manufacturer Information

Name

UreSil, LLC

Address

5418 W Touhy Ave

Skokie, Illinois, United States

Created Date

Aug 18, 2021

Authorized Representative

Name

Emergo Consulting (UK) Limited

Relationship Type

UK Responsible Person

Address

Compass House, Vision Park Histon c/o Cr360 – UL International

Cambridge, England, United Kingdom

Postcode: CB24 9BZ

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Nephrostomy catheter - UK MHRA Medical Device Registration

Device Type

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Type

Date Registered

Last Updated

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Address

Created Date

Name

Relationship Type

Address

DJ Fang

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